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Remote Cra Jobs (NOW HIRING)

Systimmune

Clinical Research Associate II

Princeton, NJ · Remote

$80K - $110K/yr

The CRA II is responsible for the management and oversight of their assigned clinical study sites ... and remote monitoring visits. * Excellent verbal and written communication skills required.

ICON

Senior CRA

Kansas City, MO · On-site +1

Senior CRA ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation ...

Icon plc

Contract Senior CRA

Portland, OR · Remote

CONTRACT SENIOR CRA/CRA II (Home-based anywhere in the U.S.) ICON is a global healthcare ... MM2 #LI-Remote Employment with ICON is contingent upon having the legal right to work in the ...

Icon plc

Contract Senior CRA

Salt Lake City, UT · Remote

CONTRACT SENIOR CRA/CRA II (Home-based anywhere in the U.S.) ICON is a global healthcare ... MM2 #LI-Remote Employment with ICON is contingent upon having the legal right to work in the ...

Icon plc

Contract Senior CRA

Blue Bell, PA · Remote

CONTRACT SENIOR CRA/CRA II (Home-based anywhere in the U.S.) ICON is a global healthcare ... MM2 #LI-Remote Employment with ICON is contingent upon having the legal right to work in the ...

ICON

Senior CRA

Long Beach, CA · On-site +1

$110K - $138K/yr

Senior CRA ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation ...

Ardelyx

In House Clinical Research Associate

Waltham, MA · On-site +1

$99K - $121K/yr

The Clinical Research Associate (CRA) supports sponsor oversight of clinical trial execution with ... Monitor site performance through centralized and remote review of study data, key performance ...

Ardelyx

In House Clinical Research Associate

Waltham, MA · On-site +1

$99K - $121K/yr

The Clinical Research Associate (CRA) supports sponsor oversight of clinical trial execution with ... Monitor site performance through centralized and remote review of study data, key performance ...

Ardelyx

In House Clinical Research Associate

Newark, CA · On-site +1

$99K - $121K/yr

The Clinical Research Associate (CRA) supports sponsor oversight of clinical trial execution with ... Monitor site performance through centralized and remote review of study data, key performance ...

Ardelyx

In House Clinical Research Associate

Newark, CA · On-site +1

$99K - $121K/yr

The Clinical Research Associate (CRA) supports sponsor oversight of clinical trial execution with ... Monitor site performance through centralized and remote review of study data, key performance ...

Ardelyx

In House Clinical Research Associate

Newark, CA · On-site +1

$99K - $121K/yr

The Clinical Research Associate (CRA) supports sponsor oversight of clinical trial execution with ... Monitor site performance through centralized and remote review of study data, key performance ...

Ardelyx

In House Clinical Research Associate

Newark, CA · On-site +1

The Clinical Research Associate (CRA) supports sponsor oversight of clinical trial execution with ... Monitor site performance through centralized and remote review of study data, key performance ...

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Remote Cra information

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$11K

$79.4K

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How much do remote cra jobs pay per year?

As of Jun 15, 2026, the average yearly pay for remote cra in the United States is $79,437.00, according to ZipRecruiter salary data. Most workers in this role earn between $33,000.00 and $136,500.00 per year, depending on experience, location, and employer.

What are Remote CRAs?

Remote Clinical Research Associates (CRAs) are professionals who monitor clinical trials and ensure compliance with regulatory requirements, study protocols, and data integrity, all while working from a remote location. Unlike traditional CRAs who travel to clinical sites, remote CRAs use technology to oversee site activities, review data, and communicate with site staff virtually. This role is essential in supporting the effective and efficient execution of clinical trials, especially as remote monitoring becomes more common in the industry.

What are the key skills and qualifications needed to thrive as a Remote Clinical Research Associate (CRA), and why are they important?

To thrive as a Remote Clinical Research Associate, you need a solid background in life sciences or a related field, experience with clinical trials, and often a bachelor's degree or higher. Familiarity with electronic data capture (EDC) systems, regulatory compliance tools, and certifications such as ACRP or SOCRA are typically required. Exceptional organizational skills, attention to detail, and clear communication are essential soft skills for effective remote monitoring and collaboration. These skills are crucial to ensure protocol adherence, data integrity, and successful coordination of clinical studies from a remote setting.

What is the difference between Remote Cra vs Remote Clinical Research Associate?

AspectRemote CraRemote Clinical Research Associate
CredentialsBachelor's degree in life sciences, clinical research experienceBachelor's degree, clinical trial knowledge, certification often preferred
Work EnvironmentHome-based, flexible schedules, virtual communicationPrimarily home-based, site visits may be required, virtual meetings common
Industry UsagePharmaceutical, biotech, CROsPharmaceutical companies, CROs, research organizations
Search & Comparison IntentYesYes

The Remote Cra and Remote Clinical Research Associate roles are similar in credentials, work environment, and industry usage. Both positions involve overseeing clinical trials remotely, requiring relevant education and experience. The main difference lies in terminology; 'Remote Cra' is often used interchangeably with 'Remote Clinical Research Associate,' but the latter may emphasize more formal certification and specific industry standards. Both roles are vital in advancing clinical research while offering flexible, remote work options.

What Does a Remote CRA Do?

The responsibilities of a remote clinical research associate (CRA) involve working to monitor research efforts and progress. During a project, the remote CRA ensures that the research team follows all necessary protocols and procedures. In this career, your responsibilities also include maintaining records of relevant data and findings and monitoring the process of the project. Since this is a remote position, you perform your duties from home or another location away from the research site. When working on a clinical drug trial or medical study, you review procedures and ensure that researchers document all necessary information to meet regulatory requirements.

What are some common challenges faced by Remote CRAs, and how can they be managed effectively?

Remote Clinical Research Associates (CRAs) often face challenges such as maintaining clear communication with on-site teams, managing multiple study sites virtually, and ensuring data integrity without in-person monitoring. To address these, successful CRAs leverage robust digital tools for documentation and communication, schedule regular virtual check-ins with site staff, and stay organized with meticulous tracking systems. Proactive problem-solving and adaptability are key to ensuring trial protocols are followed and regulatory requirements are met while working remotely.
More about Remote Cra jobs
What cities are hiring for Remote Cra jobs? Cities with the most Remote Cra job openings:
What are the most commonly searched types of Cra jobs? The most popular types of Cra jobs are:
What states have the most Remote Cra jobs? States with the most job openings for Remote Cra jobs include:
What job categories do people searching Remote Cra jobs look for? The top searched job categories for Remote Cra jobs are:
Remote Cra jobs near you
Infographic showing various Remote Cra job openings in the United States as of June 2026, with employment types broken down into 90% Full Time, 3% Part Time, and 7% Contract. Highlights an 100% Remote job distribution, with an average salary of $79,437 per year, or $38.2 per hour.
Clinical Research Associate II

Clinical Research Associate II

SystImmune, Inc

Princeton, NJ • On-site, Remote

$80K - $110K/yr

Full-time

Posted 25 days ago

Job description

SystImmune is seeking a high quality, ambitious and experienced Clinical Research Associate II (CRA II) to support SystImmune's clinical trials. The CRA II is responsible for the management and oversight of their assigned clinical study sites to ensure data quality and patient safety in accordance with ICH-GCP guidelines, local regulations, and applicable SOPs. The CRA II must be self-motivated, independent, and able to work in a small team environment. The successful candidate will be a highly organized individual who can also multitask and adjust direction based on changing project/corporate priorities.
Job Responsibilities:
  • Perform Site Evaluation Visits, Site Initiation Visits, Interim monitoring visits and Close Out Visits
  • Prepare the study reference manual, including liaising with the Contract Research Organization (CRO) team (i.e., central lab, specialty labs and vendors) to ensure efficient preparation and delivery of study materials to investigator sites
  • Responsible for ensuring investigator sites have met all contractual and regulatory requirements for site initiation and first release of study drug
  • Assist in the development of study/program plans (i.e., Monitoring Plan, eCRF Completion Guidelines, Data Management Plan, Safety Management Plan, etc.)
  • Manage patient recruitment strategies, proactively identifying barriers to recruitment while proposing solutions (i.e., study-site webinars, newsletters or other potential creative solutions)
  • Monitor recruitment, data quality and patient safety while on site and remotely through EDC systems and direct site communication
  • Liaise with study site personnel to ensure timely and correct entry of data into eCRF, including the timely resolution of data queries
  • Maintain project files including ethics committee approvals, curricula vitae of investigators and study personnel, clinical investigators brochure, protocols, case report forms instructions, consent documents, clinical-trial material shipping orders, start-up meeting attendance documentation, letters of agreement, lab reference ranges, and all investigator and site correspondence
  • Identify and complete follow- up of SAEs at study sites
  • Assist with data listing, data coding, patient profile reviews, database lock, and site close-out activities
  • Ensure appropriate and timely submission of documents to the Trial Master File
  • Perform investigational product (IP) inventory, reconciliation and reviews storage and security. Verifies the IP has been dispensed and administered to subjects/patients according to the protocol. Verifies issues or risks associated with blinded or randomized information related to IP.

Qualifications:
  • Bachelor's degree in health science or related field.
  • 2+ years monitoring Oncology trials independently conducting on-site and remote monitoring visits.
  • Excellent verbal and written communication skills required.
  • Excellent organizational, multi-tasking and time management skills required.
  • Demonstrated experience developing/maintaining site relationships and securing compliance
  • Working knowledge of International Conference on Harmonization Good Clinical Practice guidelines
  • Experienced in Microsoft Office Products (Word, Excel, PowerPoint, SharePoint, Teams) and other clinical trial systems (e.g., CTMS, EDC and eTMF)
  • Ability to travel as required (50-75%)

Compensation and Benefits:
The expected base salary range for this position is $80,000 - $110,000 annually. Actual compensation will be based on a variety of factors, including but not limited to a candidate's qualifications, experience, and skills.

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